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Procedure
3D Knee Kinematics Assessment for Understanding Knee Movement
N/A
Waitlist Available
Led By Frédéric Lavoie, MD MSc FRCSC
Research Sponsored by Centre hospitalier de l'Université de Montréal (CHUM)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients awaiting knee arthroscopy under local anesthesia for a medial meniscal tear
Must not have
Knee flexion contracture
Inability to perform the various motor tasks required by the study protocol
Timeline
Screening 3 weeks
Treatment Varies
Follow Up on the day of the surgery, before knee arthroscopy
Awards & highlights
No Placebo-Only Group
Summary
This trial will test a new system that can measure 3D knee kinematics during physical and daily activities. The hope is that this will help understand the knee joint better and why it is often injured.
Who is the study for?
This trial is for patients who are scheduled for knee arthroscopy due to a medial meniscal tear and can move their knee well enough to do certain tasks. People with active infections, severe knee swelling, stiff knees that can't bend fully, or those who limp heavily cannot participate.
What is being tested?
The study is testing a new system that uses personalized 3D bone imaging and a device attached to the bone through the skin under local anesthesia. It aims to precisely measure how the knee moves during physical activities and daily life.
What are the potential side effects?
Potential side effects may include discomfort at the site where the device attaches to the bone, bruising from needle insertion under local anesthesia, and temporary pain or swelling after performing activity tasks.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am waiting for a knee surgery under local anesthesia for a tear in my knee's inner cartilage.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I cannot fully straighten my knee.
Select...
I cannot perform the physical activities required by the study.
Select...
I have a noticeable limp.
Select...
I currently have an infection.
Select...
I have severe knee swelling.
Select...
I can't bend my knee fully.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ on the day of surgery, before knee arthroscopy
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~on the day of surgery, before knee arthroscopy
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
3D knee kinematics
Secondary study objectives
Correlation of kinematic data with clinical laxity tests
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: 3D knee kinematic assessmentExperimental Treatment1 Intervention
3D knee kinematic assessment under local anesthesia
Find a Location
Who is running the clinical trial?
Centre hospitalier de l'Université de Montréal (CHUM)Lead Sponsor
380 Previous Clinical Trials
131,579 Total Patients Enrolled
1 Trials studying 3D Knee Kinematics
30 Patients Enrolled for 3D Knee Kinematics
Eiffel MedtechIndustry Sponsor
1 Previous Clinical Trials
30 Total Patients Enrolled
1 Trials studying 3D Knee Kinematics
30 Patients Enrolled for 3D Knee Kinematics
Frédéric Lavoie, MD MSc FRCSCPrincipal InvestigatorCHUM
1 Previous Clinical Trials
140 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I cannot fully straighten my knee.I cannot perform the physical activities required by the study.I have a noticeable limp.I currently have an infection.I have severe knee swelling.I can't bend my knee fully.I am waiting for a knee surgery under local anesthesia for a tear in my knee's inner cartilage.
Research Study Groups:
This trial has the following groups:- Group 1: 3D knee kinematic assessment
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.